Abstract
Twenty-two cases of terminal deletions of the long arm of chromosome 7 have been reported. We present 5 new cases, 3 of which were ascertained due to fetal holoprosencephaly, one due to anencephaly, and one due to multiple structural defects in a 15-year-old boy. The presence of holoprosencephaly in 3 of the 5 cases reported herein and in 2 previously reported cases suggests that this manifestation may be commonly observed in individuals with deletion 7q.
Original language | English (US) |
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Pages (from-to) | 53-55 |
Number of pages | 3 |
Journal | American journal of medical genetics |
Volume | 36 |
Issue number | 1 |
DOIs | |
State | Published - 1990 |
Keywords
- holoprosencephaly
ASJC Scopus subject areas
- Genetics(clinical)